Nonalcoholic Steatohepatitis Is Associated with Altered Hepatic MicroRNA Expression

被引:549
作者
Cheung, Onpan [1 ]
Puri, Puneet [1 ]
Eicken, Christoph [4 ]
Contos, Melissa J. [3 ]
Mirshahi, Faridoddin [1 ]
Maher, James W. [2 ]
Kellum, John M. [2 ]
Min, Haeki [1 ]
Luketic, Velimir A. [1 ]
Sanyal, Arun J. [1 ]
机构
[1] Virginia Commonwealth Univ, Med Ctr, Dept Internal Med, Div Gastroenterol Hepatol & Nutr, Richmond, VA USA
[2] Virginia Commonwealth Univ, Med Ctr, Dept Surg, Richmond, VA USA
[3] Virginia Commonwealth Univ, Med Ctr, Dept Pathol, Richmond, VA USA
[4] LC Sci, Houston, TX USA
基金
美国国家卫生研究院;
关键词
D O I
10.1002/hep.22569
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The expression of microRNA in nonalcoholic steatohepatitis (NASH) and their role in the genesis of NASH are not known. The aims of this study were to: (1) identify differentially expressed microRNAs in human NASH, (2) tabulate their potential targets, and (3) define the effect of a specific differentially expressed microRNA, miR-122, on its targets and compare these effects with the pattern of expression of these targets in human NASH. The expression of 474 human microRNAs was compared in subjects with the metabolic syndrome and NASH versus controls with normal liver histology. Differentially expressed microRNAs were identified by the mu Paraflo microRNA microarray assay and validated using quantitative real-time polymerase chain reaction (PCR). The effects of a specific differentially expressed miRNA (miR-122) on its predicted targets were assessed by silencing and overexpressing miR-122 in vitro. A total of 23 microRNAs were underexpressed or overexpressed. The predicted targets of these microRNAs are known to affect cell proliferation, protein translation, apoptosis, inflammation, oxidative stress, and metabolism. The miR-122 level was significantly decreased in subjects with NASH (63% by real-time PCR, P < 0.00001). Silencing miR-122 led to an initial increase in mRNA levels of these targets (P < 0.05 for all) followed by a decrease by 48 hours. This was accompanied by an increase in protein levels of these targets (P < 0.05 for all). Overexpression of miR-122 led to a significant decrease in protein levels of these targets. Conclusions: NASH is associated with altered hepatic microRNA expression. Underexpression of miR-122 potentially contributes to altered lipid metabolism implicated in the pathogenesis of NASH. (HEPATOLOGY 2008;48: 1810-1820.)
引用
收藏
页码:1810 / 1820
页数:11
相关论文
共 31 条
  • [1] The histological course of nonalcoholic fatty liver disease: a longitudinal study of 103 patients with sequential liver biopsies
    Adams, LA
    Sanderson, S
    Lindor, KD
    Angulo, P
    [J]. JOURNAL OF HEPATOLOGY, 2005, 42 (01) : 132 - 138
  • [2] MicroRNA functions in animal development and human disease
    Alvarez-Garcia, I
    Miska, EA
    [J]. DEVELOPMENT, 2005, 132 (21): : 4653 - 4662
  • [3] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [4] A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
    Bolstad, BM
    Irizarry, RA
    Åstrand, M
    Speed, TP
    [J]. BIOINFORMATICS, 2003, 19 (02) : 185 - 193
  • [5] Chang Jinhong, 2004, RNA Biol, V1, P106, DOI 10.4161/rna.1.2.1066
  • [6] Microarray analyses of newborn mouse ovaries lacking Nobox
    Choi, Youngsok
    Qin, Yingying
    Berger, Michael F.
    Ballow, Daniel J.
    Bulyk, Martha L.
    Rajkovic, Aleksandar
    [J]. BIOLOGY OF REPRODUCTION, 2007, 77 (02) : 312 - 319
  • [7] Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III)
    Cleeman, JI
    Grundy, SM
    Becker, D
    Clark, LT
    Cooper, RS
    Denke, MA
    Howard, WJ
    Hunninghake, DB
    Illingworth, DR
    Luepker, RV
    McBride, P
    McKenney, JM
    Pasternak, RC
    Stone, NJ
    Van Horn, L
    Brewer, HB
    Ernst, ND
    Gordon, D
    Levy, D
    Rifkind, B
    Rossouw, JE
    Savage, P
    Haffner, SM
    Orloff, DG
    Proschan, MA
    Schwartz, JS
    Sempos, CT
    Shero, ST
    Murray, EZ
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19): : 2486 - 2497
  • [8] Actin-dependent intranuclear repositioning of an active gene locus in vivo
    Dundr, Miroslav
    Ospina, Jason K.
    Sung, Myong-Hee
    John, Sam
    Upender, Madhvi
    Ried, Thomas
    Hager, Gordon L.
    Matera, A. Gregory
    [J]. JOURNAL OF CELL BIOLOGY, 2007, 179 (06) : 1095 - 1103
  • [9] Cluster analysis and display of genome-wide expression patterns
    Eisen, MB
    Spellman, PT
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) : 14863 - 14868
  • [10] miR-122 regulation of lipid metabolism revealed by in vivo antisense targeting
    Esau, C
    Davis, S
    Murray, SF
    Yu, XX
    Pandey, SK
    Pear, M
    Watts, L
    Booten, SL
    Graham, M
    McKay, R
    Subramaniam, A
    Propp, S
    Lollo, BA
    Freier, S
    Bennett, CF
    Bhanot, S
    Monia, BP
    [J]. CELL METABOLISM, 2006, 3 (02) : 87 - 98